Term Name:	Holoprosencephaly 13, X-linked
Synonyms:
Definition:	A holoprosencephaly characterized by midline developmental defects that mainly affect the brain and craniofacial structure that has_material_basis_in heterozygous mutation in the STAG2 gene on chromosome Xq25.
Ontology:	Human Disease [DOID:0060954]   ( DOID:0060954 )